Double aneuploidy 48,ХХХ,+21 of a Bulgarian newborn with Down phenotype: a case report

Abstract

Background

Aneuploidy is one of the most important chromosomal aberrations, which involves an abnormal number of the chromosomes. Trisomy 21 (Down syndrome) and numerical aberrations of the sex chromosomes have a relatively high prevalence in the general population. However, the patients usually have one of the above genetic disorders and combined cases of two different trisomies are unusual.

Case presentation

We report a case of a patient with double aneuploidy—a combination of trisomy 21 and triple X syndrome. The proband had typical features of Down syndrome and did not manifest any symptoms of polysomy X. The patient had hypotonia, a cardiac defect, and an annular pancreas. A clinical diagnosis of Down syndrome was established, but the cytogenetic analysis found two free full trisomies—trisomy 21 (Down syndrome) and triple X.

Conclusion

Cases of double aneuploidy, combining trisomy 21 and trisomy of a sex chromosome, could be challenging because the patients manifest only symptoms, typical for Down syndrome. The discovery of a second complete free trisomy X in our case was an incidental finding. This illustrates the importance of the cytogenetic analysis, despite the evident phenotype of trisomy 21.

Background

Double aneuploidy (DA) is a rare genetic phenomenon in humans, and the majority of cases are found in abortive material [1]. It usually involves an autosomal trisomy such as trisomy 21, 18, or 13 and aneuploidy of the sex chromosomes. The last one could be Klinefelter, Turner syndrome, polysomy X, or polysomy Y [2]. There are also reported mosaic cases of DA, which may include other autosomes such as chromosome 8 or 14 [3, 4]. The clinical presentation of every case would be different, depending on the cytogenetic finding.

In this study, we present a case of a full free double aneuploidy, combining both trisomy 21 and triple X syndrome, described for the first time in Bulgaria.

Case presentation

The patient was a preterm girl, born in 37 gestational weeks per vias naturales after a second uneventful pregnancy. The mother’s age was 25 years old. The pregnancy was not followed-up by an obstetrician.

The birth weight of the patient was 2470 g (17.3rd percentile), birth length 46 cm (10.3rd percentile), head circumference 30 cm (2.3rd percentile). Apgar score was 5 points in 1 min and 6 points in 5 min.

The baby girl presented with upslanting palpebral fissures, and the ears were low set and with abnormal outer morphology (Fig. 1). She also showed a tendency for tongue protrusion. The patient had hypotonia. The above described dysmorphic features were suspicious for the presence of Down syndrome.

Fig. 1
figure1

Phenotype of the proband, presenting with hypotonia

А chest X-ray of the baby was done due to а systolic murmur. The X-ray showed a normal-sized cardiac silhouette and a dislocated to the right shadow of the right ventricle. A ventricular and an atrial septal defect were diagnosed after a transthoracic ultrasound of the chest. The patient had tachypnea, two-sided vesicular breathing with crepitations. The child needed a constant supply of oxygen.

Every time after the baby was fed, it vomited stomach content, and it could not gain weight. A barium X-ray examination of the abdomen was done, and it was diagnosed with a possible stenosis of the pylorus or the duodenum. On the 7th day after birth, the girl underwent a surgical correction for annular pancreas, which was constricting the duodenum. The other internal organs, bone, and soft tissues were normal.

A blood sample for cytogenetic analysis was collected to prove the clinical diagnosis of trisomy 21. The patient was discharged from the hospital and was clinically improved. The family was referred to genetic counseling.

Cytogenetic analysis of peripheral lymphocytes was performed using Giemsa staining in the Laboratory of Medical Genetics, Varna. An informed consent was received from the family. A pathological karyotype 48,ХХХ,+21 was observed in all 100 analyzed metaphase spreads. There were two additional copies of the Х chromosome and chromosome 21 (Fig. 2). The proband was diagnosed with double aneuploidy and two free full trisomies—trisomy 21 (Down syndrome) and triple X syndrome. Cytogenetic analysis of the parents was not performed.

Fig. 2
figure2

Gimsa-banded metaphase chromosomes of the patient: 48, XXX, +21. Circles indicate the additional copies of chromosome 21 and X chromosome

Discussion

The first published case of the same type of double aneuploidy—trisomy 21 together with triple X syndrome was in 1962 by Breg et al. [5]. We summarized 12 other reported cases through the years (Table 1). Even though the individual frequency of the described aneuploidy is not clear, it is estimated that the frequency of DA in general is around 0.05% in newborns [14]. Despite this, the incidence of these cases could be higher than expected, if it is multiplied by the individual frequency of each of these aneuploidies [12].

Table 1 Review of cases, combining trisomy 21 and polysomy X

The clinical presentation of patients with DA could be different, depending on the cell line, which prevails, the degree of mosaicism, and the type of affected chromosomes. There could be a combination of symptoms, typical for both observed chromosomal aberrations [1, 16]. However, DA of trisomy 21 and a sex chromosome aneuploidy is an exception since there are usually phenotypic traits only of Down syndrome. This is because trisomies of the sex chromosomes generally do not manifest with facial dysmorphism or congenital anomalies [17].

This is also observed in our case due to the fact that triple X syndrome is not associated with any clinical severe features [18]. The main symptoms of our patient are due to the additional copy of chromosome 21. Nevertheless, in cases of triple X syndrome, there may be a developmental delay, learning disabilities, speech problems, behavioral, emotional disorders, and delayed motor skills. Also, there could be menstrual disturbances and early menopause [19]. This illustrates the importance of regular follow-up of our patient with DA not only for complications due to trisomy 21, but also because of the additional copy of the X chromosome.

In contrast to polysomy X, dysmorphic features of monosomy X could be present right after the birth of the baby—for example, lymphedema of hands and feet [20]. However, in cases of mosaicism for the Turner syndrome, the dysmorphic features of Down syndrome would be the main reason for genetic testing [21]. That is why cytogenetic analysis is always required to check for other chromosomal aberrations.

Double aneuploidies are the result of nondisjunction of the chromosomes during the meiotic or mitotic division, but the last one would lead to somatic mosaicism. In cases of meiotic nonreduction, the parental origin of the additional genetic material depends on the time of the nondisjunction [13, 14]. If it occurs during meiosis I, the newly formed gamete will have 24 chromosomes in total and there will be both a maternal and a paternal copy of the additional chromosome. If the homologous chromosomes do not separate during meiosis II, the gamete will have again 24 chromosomes, but the extra one will have the same parental origin—either maternal or paternal. Both of the described aneuploidies in cases of double aneuploidy could have the same or different parental background [13]. However, in around 85.00% of the cases the additional chromosome 21 is maternal. The parental contribution for the additional X chromosome is equal [22].

In most of the cases described in the literature, it was concluded that the DA, no matter if it is trisomy and/or monosomy of two different chromosomes, resulted from the nondisjunction of the chromosomes during the second mitotic division [13, 23, 24]. The failure of the sister chromatids to separate during the cell division (mitosis or meiosis) is relatively common, especially during ovogenesis, and it is not so typical for spermatogenesis. There are no certain risk factors or specific mutations, which are associated with a greater chance of nondisjunction. The most important risk factor is advanced maternal age over 35 years old [18]. However, in our case, the maternal age is not increased—it is 25 years.

Also, monosomies of the autosomes are not compatible with life. Only X monosomies could result in a live birth [1, 14]. Having an additional genetic material is better tolerated possibly due to dosage compensation mechanisms [25]. That is why most of the published cases of DAs, which did not end with the death of the embryo, had for example trisomies. The most common DAs involve chromosome 21, followed by chromosome 16, X, 22, 18, 13, and 15 in a descending order. The combination of Down and Klinefelter syndromes occurs with the highest prevalence in live births [26]. However, the main etiological factors, responsible for double aneuploidies, are unknown [12]. In order to examine the possible mechanism of nondisjunction, it is recommended to check the parental origin of each of the additional chromosomes [24]. This was not done in the case described because of the parents’ refusal, and we were unable to identify the mechanism of the DA. The mother of our patient denied any exposure to teratogenic agents during pregnancy, and there was no history of other cases of chromosomal aberrations in the family (for example, other children with Down syndrome) and the maternal age was not advanced. That is why it is difficult to presume what were the etiological factors for double aneuploidy in the case described.

No matter the etiology of the DA, the change in the number of the chromosomes could be detected by using non-invasive prenatal testing [27]. However, the finding must be confirmed by chorionic villus sampling or amniocentesis because there might be another cause for the DA, for example, placental mosaicism or an underlying maternal disease [28]. The genetic counseling in these cases could be very challenging because of the possible discordance of the result and the actual karyotype of the patient.

Conclusions

The presented case of double aneuploidy could be a challenging diagnosis because the patient manifested only symptoms, typical for Down syndrome. The discovery of a second complete free trisomy X was an incidental finding. That is why it is recommended to order a cytogenetic analysis in every case of Down syndrome, despite the evident phenotype of trisomy 21. This type of genetic testing would not only confirm the diagnosis, but it would also exclude additional chromosomal aberration, like double aneuploidies.

Availability of data and materials

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Abbreviations

DA:

Double aneuploidy

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Authors

Contributions

M.T. conducted the analysis and drafted the work. M.L. revised the manuscript and consulted the patients. S.T. is the neonatologist, who took care of the patient. M. H. helped with the laboratory work and the genetic counseling. E.K. provided key information and helped revise the manuscript. L.A. supervised the work process and revised the manuscript. All authors commented on previous versions of the manuscript. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Mariya Levkova.

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Tsvetkova, M., Levkova, M., Tsvetkova, S. et al. Double aneuploidy 48,ХХХ,+21 of a Bulgarian newborn with Down phenotype: a case report. Egypt J Med Hum Genet 21, 25 (2020). https://doi.org/10.1186/s43042-020-00068-2

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Keywords

  • Double aneuploidy
  • Down syndrome
  • Triple X syndrome
  • Case report